Canonical Allele Identifier: CA531391285

Gene: HADHA GAREM2

Linked Data

• dbSNP Id: rs367911534
• gnomAD v2: 2-26414073-C-A
• gnomAD v4: 2-26191204-C-A
• MyVariant Identifiers: chr2:g.26414073C>A (hg19) ; chr2:g.26191204C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26191204C>A , CM000664.2:g.26191204C>A	GRCh38
NC_000002.11:g.26414073C>A , CM000664.1:g.26414073C>A	GRCh37
NC_000002.10:g.26267577C>A	NCBI36
NG_007121.1:g.58417G>T
NG_007121.2:g.58418G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.*46G>T (HADHA) MANE Select	ENSP00000370023.3:n.*46G>T
ENST00000492433.2:c.*46G>T (HADHA)	ENSP00000438039.2:n.*46G>T
ENST00000643057.1:c.*2316G>T (HADHA)	ENSP00000493761.1:n.*2316G>T
ENST00000643063.1:c.*1384G>T (HADHA)	ENSP00000495353.1:n.*1384G>T
ENST00000643233.1:c.*2229G>T (HADHA)	ENSP00000493880.1:n.*2229G>T
ENST00000644428.1:c.*962G>T (HADHA)	ENSP00000495560.1:n.*962G>T
ENST00000645274.1:c.*46G>T (HADHA)	ENSP00000493996.1:n.*46G>T
ENST00000646031.1:c.1697G>T (HADHA)
ENST00000380649.7:c.*46G>T (HADHA)	ENSP00000370023.3:n.*46G>T
NM_000182.4:c.*46G>T (HADHA)	NP_000173.2:n.*46G>T
XM_011532567.1:c.1683+3889C>A (GAREM2)	XP_011530869.1:n.1683+3889C>A
XM_011532567.3:c.1683+3889C>A (GAREM2)	XP_011530869.1:n.1683+3889C>A
NM_000182.5:c.*46G>T (HADHA) MANE Select	NP_000173.2:n.*46G>T